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Inactivation of HCoV-NL63 and SARS-CoV-2 in aqueous solution by 254 nm UV-C.
Li, Lily X; Nissly, Ruth H; Swaminathan, Anand; Bird, Ian M; Boyle, Nina R; Nair, Meera Surendran; Greenawalt, Denver I; Gontu, Abhinay; Cavener, Victoria S; Sornberger, Ty; Freihaut, James D; Kuchipudi, Suresh V; Bahnfleth, William P.
Affiliation
  • Li LX; Pennsylvania State University, Department of Architectural Engineering, 104 Engineering Unit A, University Park, PA, 16802, United States of America.
  • Nissly RH; Pennsylvania State University, Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, University Park, PA 16802, United States of America.
  • Swaminathan A; Pennsylvania State University, Department of Architectural Engineering, 104 Engineering Unit A, University Park, PA, 16802, United States of America.
  • Bird IM; Pennsylvania State University, Huck Institutes of the Life Sciences, University Park, PA 16802, United States of America.
  • Boyle NR; Pennsylvania State University, Huck Institutes of the Life Sciences, University Park, PA 16802, United States of America.
  • Nair MS; Pennsylvania State University, Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, University Park, PA 16802, United States of America.
  • Greenawalt DI; Pennsylvania State University, Huck Institutes of the Life Sciences, University Park, PA 16802, United States of America.
  • Gontu A; Pennsylvania State University, Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, University Park, PA 16802, United States of America.
  • Cavener VS; Pennsylvania State University, Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, University Park, PA 16802, United States of America.
  • Sornberger T; Pennsylvania State University, Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, University Park, PA 16802, United States of America.
  • Freihaut JD; Pennsylvania State University, Department of Architectural Engineering, 104 Engineering Unit A, University Park, PA, 16802, United States of America. Electronic address: jdf11@psu.edu.
  • Kuchipudi SV; Pennsylvania State University, Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, University Park, PA 16802, United States of America; Pennsylvania State University, Huck Institutes of the Life Sciences, University Park, PA 16802, United States of America. Electronic add
  • Bahnfleth WP; Pennsylvania State University, Department of Architectural Engineering, 104 Engineering Unit A, University Park, PA, 16802, United States of America. Electronic address: wpb5@psu.edu.
J Photochem Photobiol B ; 245: 112755, 2023 Aug.
Article in En | MEDLINE | ID: mdl-37423001
ABSTRACT
Ultraviolet germicidal irradiation (UVGI) is a highly effective means of inactivating many bacteria, viruses, and fungi. UVGI is an attractive viral mitigation strategy against coronaviruses, including the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the cause of the coronavirus disease-2019 (COVID-19) pandemic. This investigation measures the susceptibility of two human coronaviruses to inactivation by 254 nm UV-C radiation. Human coronavirus NL63 and SARS-CoV-2 were irradiated in a collimated, dual-beam, aqueous UV reactor. By measuring fluence and integrating it in real-time, this reactor accounts for the lamp output transients during UVGI exposures. The inactivation rate constants of a one-stage exponential decay model were determined to be 2.050 cm2/mJ and 2.098 cm2/mJ for the NL63 and SARS-CoV-2 viruses, respectively. The inactivation rate constant for SARS-CoV-2 is within 2% of that of NL63, indicating that in identical inactivation environments, very similar UV 254 nm deactivation susceptibilities for these two coronaviruses would be achieved. Given the inactivation rate constant obtained in this study, doses of 1.1 mJ/cm2, 2.2 mJ/cm2, and 3.3 mJ/cm2 would result in a 90%, 99%, and 99.9% inactivation of the SARS-CoV-2 virus, respectively. The inactivation rate constant obtained in this study is significantly higher than values reported from many 254 nm studies, which suggests greater UV susceptibility to the UV-C than what was believed. Overall, results from this study indicate that 254 nm UV-C is effective for inactivation of human coronaviruses, including SARS-CoV-2.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Photochem Photobiol B Journal subject: BIOLOGIA Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Photochem Photobiol B Journal subject: BIOLOGIA Year: 2023 Type: Article Affiliation country: United States